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通过改良的聚合酶链反应产物高分辨率熔解曲线分析法检测结核分枝杆菌pncA基因中的突变

Detection of Mutations in Mycobacterium tuberculosis pncA Gene by Modified High-Resolution Melting Curve Analysis of PCR Products.

作者信息

Filipenko M L, Dymova M A, Cherednichenko A G, Khrapov E A, Mishukova O V, Schwartz Ya Sh

机构信息

Institute of Chemical Biology and Fundamental Medicine, Siberian Division of the Russian Academy of Sciences, Novosibirsk, Russia.

Novosibirsk Research Institute of Tuberculosis, Ministry of Health of the Russian Federation, Novosibirsk, Russia.

出版信息

Bull Exp Biol Med. 2019 Dec;168(2):264-269. doi: 10.1007/s10517-019-04688-6. Epub 2019 Nov 28.

Abstract

We developed a protocol for detection of mutations in the pncA gene associated with M. tuberculosis resistance to pyrazinamide by analyzing melting curves of 7 overlapping amplicons with artificial heteroduplex formation (H-HRM) formed by co-amplification of wild-type DNA and test DNA and compared its efficiency and robustness with those of classical HRM analysis. Using HRM and H-HRM, we analyzed 35 PZA DNA isolates carrying mutations in the pncA gene, 3 PZA isolates without mutations in the pncA gene, and 20 PZA isolates without mutations in the pncA gene were analyzed. The sensitivity and specificity of HRM for detection of mutations in the pncA gene were moderate: 88.57% (CI 73.26%-96.80%) and 82.61% (CI 61.22%-95.05%), respectively. The sensitivity of the H-HRM test was 97.14% (CI 85.08%-99.93%) and specificity was 95.65% (CI 78.05%-99.89%), with a significant improvement in accuracy - 96.55% vs. 93.85% for HRM. In general, despite addition stage of equalizing the concentrations of the test and control mycobacterial DNA, H-HRM showed greater stability and reproducibility at standard settings of the melting curve analysis software.

摘要

我们开发了一种通过分析7个重叠扩增子的熔解曲线来检测与结核分枝杆菌对吡嗪酰胺耐药性相关的pncA基因突变的方案,该方案通过野生型DNA和测试DNA的共扩增形成人工异源双链(H-HRM),并将其效率和稳健性与经典的高分辨率熔解曲线分析(HRM)进行了比较。使用HRM和H-HRM,我们分析了35个携带pncA基因突变的吡嗪酰胺(PZA)DNA分离株、3个pncA基因无突变的PZA分离株以及20个pncA基因无突变的PZA分离株。HRM检测pncA基因突变的敏感性和特异性中等:分别为88.57%(95%置信区间73.26%-96.80%)和82.61%(95%置信区间61.22%-95.05%)。H-HRM检测的敏感性为97.14%(95%置信区间85.08%-99.93%),特异性为95.65%(95%置信区间78.05%-99.89%),准确性有显著提高——HRM为93.85%,H-HRM为96.55%。总体而言,尽管增加了使测试和对照分枝杆菌DNA浓度相等的步骤,但在熔解曲线分析软件的标准设置下,H-HRM显示出更高的稳定性和可重复性。

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